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New treatment option for Missing Tooth
Official title Peri-implant Soft Tissue Response to Direct Zirconia-Based Composite Customized Healing Abutment
ClinicalTrials.gov ID: NCT07095881
What this study is testing
- What it's testing
- The goal of this clinical trial is to learn if using zirconia-based composite customized healing abutment can have a favorable effect on peri implant soft tissue that may be related to the superior biological properties of zirconium nano particles regarding increased biocompatibility and decreased inflammatory response Patients that are eligible for implant placement The main question it aims to answer is: Does zirconia-based composite customized healing abutment have a significantly different effect on peri-implant soft tissue compared to conventional composite customized healing abutment in terms of biological properties or biocompatibility or inflammatory response? Researchers will compare between direct zirconia-based composite customized healing abutments vs conventional composite customized healing abutments placed simultaneously with delayed dental implant placement.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 20 to 50
You may be able to join if
- Patients should be systematically free from any disease as according to Cornell Medical Index-Health Questionnaire (Pendleton et al., 2004).
- Both genders.
- Age from 20-50 years.
- Missing tooth to be restored with standard implant, with no need for additional bone and soft tissue augmentation procedures (Beretta et al., 2019).
- Implants primary stability ISQ ≥ 70 unites using the Osstell Mentor (Baltayan et al., 2016).
You likely can't join if
- Poor oral hygiene condition.
- Pregnant and lactating females.
- Smokers.
- Vulnerable groups (Prisoners and handicaps).
See the full eligibility criteria
- Patients should be systematically free from any disease as according to Cornell Medical Index-Health Questionnaire (Pendleton et al., 2004).
- Both genders.
- Age from 20-50 years.
- Missing tooth to be restored with standard implant, with no need for additional bone and soft tissue augmentation procedures (Beretta et al., 2019).
- Implants primary stability ISQ ≥ 70 unites using the Osstell Mentor (Baltayan et al., 2016).
- Sound Mesial and distal neighboring teeth.
- At least 6 natural teeth remaining in the same arch .
- Mouth opening ≥ 30mm.
- Thick phenotype.
- Poor oral hygiene condition.
- Pregnant and lactating females.
- Smokers.
- Vulnerable groups (Prisoners and handicaps).
The study team makes the final eligibility decision.
Where it's taking place
- Cairo, Abaseya, Egypt
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 20 years to 50 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Cairo, Abaseya, Egypt. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.